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US8354093B2ExpiredUtilityPatentIndex 79

Cell permeable nanoconjugates of shell-crosslinked knedel (SCK) and peptide nucleic acids (“PNAs”) with uniquely expressed or over-expressed mRNA targeting sequences for early diagnosis and therapy of cancer

Assignee: UNIV WASHINGTONPriority: Oct 15, 2004Filed: Oct 14, 2005Granted: Jan 15, 2013
Est. expiryOct 15, 2024(expired)· nominal 20-yr term from priority
Inventors:BECKER MATTHEW LFANG HUAFENGLI XIAOXUPAN DIPANJANROSSIN RAFFAELLASUN XIANKAITAYLOR JOHN-STEPHENTURNER JEFFREY LWELCH MICHAEL JOHNWOOLEY KAREN L
C12N 2310/3513A61K 51/1251B82Y 30/00C12N 2310/11C12N 2310/3231B82Y 5/00C12N 2320/31C12N 15/111C12N 2310/321C12N 2320/10C12N 15/1135C01P 2004/64C12N 2310/3517C12N 2310/3181A61K 31/7088
79
PatentIndex Score
6
Cited by
4
References
8
Claims

Abstract

A functional biologically active particle conjugate useful for diagnosis and treating cancer as a bioportal comprises a nanoscale particle having associated therewith an intracellular targeting ligand comprising a PNA, or another nuclease resistant oligonucleotide analog such as MOE-mRNA (2′-methoxyethyl mRNA) or LNA (locked nucleic acid), having a sequence that binds selectively to an uniquely expressed or overexpressed mRNA specific to the cancer or disease state in a living mammal. In one aspect the uniquely overexpressed target specific to the cancer or disease state is the unr mRNA which can be targeted by the antisense sequence PNA50.

Claims

exact text as granted — not AI-modified
1. A diagnostic target-specific imaging probe comprising an intracellular targeting ligand comprising a peptide nucleic acid, wherein the peptide nucleic acid is SEQ ID NO: 3, or a nuclease resistant oligonucleotide analog, wherein the nuclease resistant oligonucleotide analog is a MOE-mRNA of SEQ ID NO: 3 or a LNA of SEQ ID NO: 3, wherein the SEQ ID NO: 3 binds selectively to an uniquely expressed or overexpressed mRNA, wherein the uniquely expressed or overexpressed mRNA is an unr mRNA, a permeation peptide, and at least one detectably labeled compound. 
     
     
       2. A pharmaceutical kit comprising the diagnostic target-specific imaging probe of  claim 1  and a pharmaceutically acceptable carrier, excipient, diluent, or saline composition. 
     
     
       3. The diagnostic target-specific imaging probe of  claim 1 , wherein the permeation peptide is selected from the group consisting of a HIV-1 TAT protein transduction domain, KPKKKRKV, GRKKRR, and four lysine residues. 
     
     
       4. The diagnostic target-specific imaging probe of  claim 1 , wherein the at least one detectably labeled compound is selected from the group consisting of a fluorophore, a radionucleotide, and combinations thereof. 
     
     
       5. A diagnostic target-specific imaging probe comprising an intracellular targeting ligand comprising a permeation peptide, a peptide nucleic acid, wherein the peptide nucleic acid is SEQ ID NO: 3, and at least one detectably labeled compound. 
     
     
       6. The diagnostic target-specific imaging probe of  claim 5 , wherein the permeation peptide is selected from the group consisting of a HIV-1 TAT protein transduction domain, KPKKKRKV, GRKKRR, and four lysine residues. 
     
     
       7. The diagnostic target-specific imaging probe in accordance with  claim 5 , further comprising a shell crosslinked knedel shell crosslinked nanoparticle. 
     
     
       8. The diagnostic target-specific imaging probe in accordance with  claim 1 , further comprising a shell crosslinked knedel shell crosslinked nanoparticle.

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